Validation Officer Temp to Permanent (Six months) subject to extend for 6 months or convert to permanent at end of 6 months) About the Company At SFI Health, we believe we have the responsibility to bring proven natural health solutions to people’s healthcare needs. We are a global natural health company committed to sourcing and producing natural medicines to the highest standards. Backed by evidence of effectiveness, quality and safety, our products are marketed around the world using our international community of leading life sciences companies and distributor networks. You will join the business at a time of significant positive change and be able to directly contribute to the strategic goals. To find out more, please visit: https://www.sfihealth.com/about-us/our-story About the Role This role is responsible for ensuring compliance with all relevant legislation and ensuring the Quality System is fit for purpose to deliver business goals. Reporting directly to the Head of Quality, the jobholder is responsible for organization, execution, reporting and review of all aspects of validation and qualification process and activities across site including but not limited to; Equipment Facility Utility Cleaning Computer Systems Shipping Analytical methods. Responsibilities Review Site Validation Systems against GMP requirements to ensure compliance, including: Validation Master File; Asset List and equipment validations; Process validation protocol and report templates, procedures and status; Analytical Test Methods, including validation status, analytical method validation protocol and report templates; Cleaning Validation protocol and report templates; Spreadsheet validation protocol and report templates. Validate critical spreadsheets; Execute seasonal site temperature mapping; Execute seasonal transport temperature mapping; Execute stability cabinet temperature mapping; Lead ongoing validation of new equipment on site. Qualifications Scientific degree or relevant experience Required Skills Extensive knowledge of GMP environments, particularly in a pharmaceutical background. Knowledge of MHRA, FDA, and Eudra guidelines. Strong working knowledge of relevant computer systems including MS Office, Microsoft Word, Excel, SharePoint, PowerPoint, ), TrackWise and SAP. Right to work in UK Proven validation experience within a pharmaceutical manufacturing. At least 10 years working in a pharmaceutical or BRC environment, including minimum of 4 years performing validation work. Strong interpersonal skills and able to work with others or as an individual as and when required. Pay range and compensation package We understand the importance of work-life balance and are dedicated to supporting our employees' personal and professional needs. This is an exceptionally good time to join this transforming business with an ambitious roadmap. Along with. Industry-competitive salary and equity Diverse Work culture Flexi working Paid holiday Bank Holidays Company Sick pay Company Bonus Insurance Free car parking Pension Equal Opportunity Statement To all recruitment agencies: We are not looking to engage Agencies currently.